Variant #0000536632 (NC_000009.11:g.134397547G>A, NM_007171.3:c.2005G>A (POMT1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.134397547G>A
DNA change (hg38) g.131522160G>A
Published as POMT1(NM_001077365.1):c.1939G>A (p.(Ala647Thr))
ISCN -
DB-ID POMT1_000084 See all 12 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 +?/. - c.2005G>A r.(?) p.(Ala669Thr)
UCK1 NM_031432.2 +?/. - c.*2880C>T r.(=) p.(=)


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